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Synthesis of hesperetin-loaded PLGA nanoparticles by two different experimental design methods and biological evaluation of optimized nanoparticles

dc.contributor.authorDuranoglu, Dilek
dc.contributor.authorUzunoglu, Deniz
dc.contributor.authorMansuroglu, Banu
dc.contributor.authorArasoglu, Tulin
dc.contributor.authorDerman, Serap
dc.date.accessioned2026-06-27T14:13:00Z
dc.date.issued2018
dc.description.abstractHesperetin was effectively encapsulated into poly (d,l-lactic-co-glycolic acid) nanoparticles by using experimental design methods. A seven-factor Plackett-Burman design was used in order to determine the major process parameters. A significant linear equation, which shows the effect of each process parameter on encapsulation efficiency was developed, and then the most effective factors were determined. Further investigation and optimization was carried out by applying the three-factor three-level Box-Behnken design. Significant second-order mathematical models were developed by regression analysis of the experimental data for both responses: encapsulation efficiency and nanoparticle size. The two step experimental design allowed the synthesis of the desired nanoparticle formulations with maximum encapsulation efficiency (80.5 +/- 4.9%) and minimum particle size (260.2 +/- 16.5 nm) at optimum process conditions: 0.5% polyvinyl alcohol (PVA) concentration, 5.13 water: organic phase ratio, and 3.59 ml min(-1) flow rate of the emulsified solution into 0.1% PVA. Furthermore, the biological activity of these optimized nanoparticles were determined with antimicrobial activity and cytotoxicity studies; results were then compared to the free hesperetin. The cytotoxicity result revealed that hesperetin and hesperetin-loaded nanoparticles were biocompatible with normal cell line L929 fibroblast cells up to 184.83 and 190.88 mu g ml(-1) for 24 h, and up to 133.24 and 134.80 mu g ml(-1) for 48 h, respectively. In the antimicrobial study, the optimized nanoparticle showed inhibition activity (minimal inhibitory concentration (MIC) values were 125 mu g ml(-1) for Escherichia coli, and 200 mu g ml(-1) for Staphylococcus aureus), while the free hesperetin did not demonstrate activity in both strains (MIC value >200 mu g ml(-1)). These in vitro results may provide useful information for the investigation of hesperetin-loaded nanoparticles in diagnostic and therapeutic applications.en
dc.description.urihttps://doi.org/10.1088/1361-6528/aad111
dc.identifier.doi10.1088/1361-6528/aad111
dc.identifier.eissn1361-6528
dc.identifier.issn0957-4484
dc.identifier.issue39
dc.identifier.pubmed29972381
dc.identifier.urihttps://hdl.handle.net/20.500.14981/58039
dc.identifier.volume29
dc.identifier.wos000439825700001
dc.language.isoeng
dc.publisherIOP PUBLISHING LTD
dc.relation.ispartofNANOTECHNOLOGY
dc.subjectexperimental design
dc.subjectPlackett-Burman
dc.subjectBox-Behnken
dc.subjecthesperetin
dc.subjectnanoparticle
dc.subjectBIODEGRADABLE NANOPARTICLES
dc.subjectPARTICLE-SIZE
dc.subjectCITRUS FLAVONOIDS
dc.subjectDRUG-DELIVERY
dc.subjectHESPERIDIN
dc.subjectCARCINOGENESIS
dc.subjectHYDROCHLORIDE
dc.subjectFORMULATION
dc.subjectINHIBITION
dc.subjectDIOSMIN
dc.subjectScience & Technology - Other Topics
dc.subjectMaterials Science
dc.subjectPhysics
dc.titleSynthesis of hesperetin-loaded PLGA nanoparticles by two different experimental design methods and biological evaluation of optimized nanoparticles
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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